HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524601Generated: October 26, 2026
Potassium Carbonate → (2R,3S)-4-((6-(2-bromo-4-fluorophenyl)-5-(ethoxycarbonyl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)-2-methylmorpholine-3-carboxylic acid
https://huagongshe.com/reaction/524601
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2R,3S)-2-methylmorpholine-3-carboxylic acid | HCID 45791333 | — |
| Reactant | Ethyl 4-(2-bromo-4-fluorophenyl)-6-(bromomethyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate | HCID 59495567 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (2R,3S)-4-((6-(2-bromo-4-fluorophenyl)-5-(ethoxycarbonyl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)-2-methylmorpholine-3-carboxylic acid | HCID 73295804 | 45% |
Reaction Steps
A mixture of ethyl 4-(2-bromo-4-fluorophenyl)-6-(bromomethyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (0.96 g, 1.9 mmol), (2R,3S)-2-methylmorpholine-3-carboxylic acid (0.28 g, 1.9 mmol) and potassium carbonate (0.53 g, 3.8 mmol) in anhydrous ethanol (35 mL) was stirred at 25° C. for 12 hours under N2. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by a silica gel column chromatography (DCM/MeOH (V/V)=15/1) to give the title compound as a yellow solid (0.48 g, 45%). The compound was characterized by the following spectroscopic data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340538B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-f023eaff99374f258b7f11e3d4aee32a |
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| Source note | uspto-grants-2016_05 |
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